This isn't a normal blog...

Life gets kinda chaotic around here... so don't expect regular posts. This blog is a gradual collection of hints, tips, and anecdotes about how we live life with one son who has autism, one daughter who is "typical", one son who is profoundly disabled and medically fragile, and one daughter with borderline delays and unclear medical complications. When life gets crazy, I won't post...but when things slow down (or I'm sitting in the hospital for a few days twiddling my thumbs) I'll add more posts about things we do to live a fun and joyful life...to the best of our abilities.


Sunday, July 1, 2012

Hotels

Most wheelchair-accessible rooms in hotels do not have enough space for our family.  They usually only have one bed.  (What, people in wheelchairs don't have families?  They always travel alone? They never travel?)
 With three kids and two parents, that won't work (and the hotel can't rent it to that many people anyway).  Since Nate doesn't use the bathroom, all we really need is accessibility to the room itself, and maneuverability inside the room.  So, we usually request a room on the ground floor or near an elevator, since we have tons of supplies and medical equipment to haul in and out of the room.  Also, most suites have more open floorspace than any typical "wheelchair-accessible" room, so a one-room suite is actually a better choice for us, when it's possible.  The suites with kitchenettes are really nice for long stays, since we can save money by cooking in the room rather than eating out.  But usually we make do with a mini-fridge (a must for Nate's meds and special formula).

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